(2E,6E)-2-(2,3-dimethoxybenzylidene)-6-(4-methylbenzylidene)cyclohexanone

ID: ALA3794580

Chembl Id: CHEMBL3794580

PubChem CID: 127032091

Max Phase: Preclinical

Molecular Formula: C23H24O3

Molecular Weight: 348.44

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  COc1cccc(/C=C2\CCC/C(=C\c3ccc(C)cc3)C2=O)c1OC

Standard InChI:  InChI=1S/C23H24O3/c1-16-10-12-17(13-11-16)14-18-6-4-7-19(22(18)24)15-20-8-5-9-21(25-2)23(20)26-3/h5,8-15H,4,6-7H2,1-3H3/b18-14+,19-15+

Standard InChI Key:  UVDKMRJOCTZURG-JSAVKQRWSA-N

Alternative Forms

  1. Parent:

    ALA3794580

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Associated Targets(Human)

U-937 (7138 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PTGS2 Tclin Cyclooxygenase-2 (13999 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

RAW264.7 (28094 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PTGS1 Cyclooxygenase-1 (5266 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: NoFirst In Class: NoBlack Box: No
Chirality: NoAvailability: NoProdrug: No

Drug Indications

MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Calculated Properties

Molecular Weight: 348.44Molecular Weight (Monoisotopic): 348.1725AlogP: 5.23#Rotatable Bonds: 4
Polar Surface Area: 35.53Molecular Species: NEUTRALHBA: 3HBD:
#RO5 Violations: 1HBA (Lipinski): 3HBD (Lipinski): #RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: CX LogP: 5.80CX LogD: 5.80
Aromatic Rings: 2Heavy Atoms: 26QED Weighted: 0.71Np Likeness Score: -0.43

References

1. Mohd Aluwi MF, Rullah K, Yamin BM, Leong SW, Abdul Bahari MN, Lim SJ, Mohd Faudzi SM, Jalil J, Abas F, Mohd Fauzi N, Ismail NH, Jantan I, Lam KW..  (2016)  Synthesis of unsymmetrical monocarbonyl curcumin analogues with potent inhibition on prostaglandin E2 production in LPS-induced murine and human macrophages cell lines.,  26  (10): [PMID:27040659] [10.1016/j.bmcl.2016.03.092]

Source